Background:

This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases| suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.

Classification:

Primary antibody

Alternative names:

WBS22

Species reactivity:

Human, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human WBS22

Concentration:

1 mg/ml

Molecular weight:

30910

Applications:

WB

Storage:

-20°C for 1 year

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